Search results for paroxysmal dyskinesia

225 hits were found for paroxysmal dyskinesia

# Family MCID Name MIFTS Score
1
FML185 Familial Paroxysmal Kinesigenic Dyskinesia 20 7.858
2
P FML186 Familial Paroxysmal Nonkinesigenic Dyskinesia 23 6.909
3
PRX090 Paroxysmal Nonkinesigenic Dyskinesia, 3, with or Without Generalized Epilepsy 19 5.781
4
CNV018 Convulsions, Familial Infantile, with Paroxysmal Choreoathetosis 34 5.597
5
c PRX088 Paroxysmal Nonkinesigenic Dyskinesia 1 23 4.613
6
P EPS030 Episodic Kinesigenic Dyskinesia 1 30 4.559
7
c PRX024 Paroxysmal Nonkinesigenic Dyskinesia 2 13 4.529
8
GLT032 Glut1 Deficiency Syndrome 2, Childhood Onset 30 3.624
9
PRX022 Paroxysmal Choreoathetosis 23 3.081
10
PRX086 Paroxysmal Exertion-Induced Dyskinesia 20 3.032
11
P PRM011 Primary Ciliary Dyskinesia 56 0.506
12
P DYS154 Dystonia 61 0.256
13
MVM001 Movement Disease 52 0.226
14
c CNT035 Central Nervous System Disease 60 0.208
15
P EPL164 Epilepsy 65 0.204
16
P HRT032 Heart Disease 75 0.192
17
ALR002 Al-Raqad Syndrome 29 0.179
18
HPT074 Hepatic Adenoma, Somatic 44 0.165
19
BSL008 Basal Ganglia Disease 44 0.158
20
P NRV007 Nervous System Disease 70 0.150
21
HNM002 Hinman Syndrome 27 0.149
22
MYL009 Myelodysplastic Syndrome 71 0.141
23
AND005 Androgen Insensitivity Syndrome, Mild 16 0.136
24
HDC001 Headache 53 0.135
25
VND001 Vein Disease 49 0.129
26
P ATX004 Ataxia 52 0.126
27
ADC005 Adcy5-Related Dyskinesia 11 0.114
28
CRB009 Cerebritis 39 0.113
29
MTH009 Mouth Disease 62 0.113
30
BRT030 Birth Defects 44 0.112
31
NLL002 Null Syndrome 26 0.108
32
P HML002 Hemolytic Anemia 61 0.107
33
NRN002 Neuronitis 39 0.101
34
PRP019 Peripheral Nervous System Disease 53 0.100
35
c PND001 Pain Disorder 55 0.100
36
CHL071 Child Syndrome 59 0.098
37
KDS001 Kid Syndrome 57 0.098
38
PHY002 Physical Disorder 43 0.097
39
WLF001 Wolff-Parkinson-White Syndrome 55 0.092
40
P ENC018 Encephalopathy 52 0.091
41
DYS140 Dyskinesia, Familial, with Facial Myokymia 23 0.088
42
ATN002 Autonomic Nervous System Disease 48 0.088
43
VST004 Vestibular Disease 43 0.086
44
SPS057 Spasticity 42 0.086
45
ISC004 Ischemia 59 0.085
46
GLT031 Glut1 Deficiency Syndrome 1, Infantile Onset, Severe 32 0.084
47
c EPS013 Episodic Kinesigenic Dyskinesia 2 17 0.084
48
P TRM003 Tremor 53 0.083
49
RTN023 Retinitis 49 0.083
50
P HMP006 Hemiplegic Migraine 44 0.080
51
c DYS119 Dystonia 9 35 0.080
52
P PSD015 Pseudohypoparathyroidism 46 0.080
53
P INT063 Intellectual Disability 58 0.079
54
HYP056 Hypoglycemia 60 0.077
55
MGR028 Migraine with or Without Aura 1 46 0.077
56
SLP005 Sleep Disorder 54 0.076
57
P THR014 Thrombocytopenia 63 0.075
58
P SZR006 Seizure Disorder 54 0.074
59
P CRD011 Cardiomyopathy 67 0.072
60
P PNM007 Pneumonia 66 0.072
61
MYC033 Myoclonus 41 0.072
62
P HPT021 Hepatitis 68 0.071
63
P EPS003 Episodic Ataxia 54 0.071
64
CSY001 C Syndrome 53 0.071
65
c BNG023 Benign Familial Infantile Epilepsy 40 0.071
66
NSL022 Nasal Cavity Disease 40 0.069
67
P MCR010 Microcephaly 58 0.067
68
P CRB042 Cerebellar Ataxia 69 0.067
69
P FNC043 Fanconi Anemia, Complementation Group E 51 0.067
70
P CRV039 Cervicitis 45 0.067
71
ADL002 Adult Syndrome 57 0.067
72
P AST005 Asthma 81 0.066
73
INS001 Insulinoma 60 0.064
74
END072 Endotheliitis 41 0.064
75
ATH004 Athetosis 26 0.064
76
P HYP086 Hypothyroidism 60 0.063
77
UND005 Undifferentiated Pleomorphic Sarcoma 44 0.063
78
CHR073 Choreatic Disease 34 0.063
79
PRX087 Paroxysomal Nonkinesigenic Dyskinesia 3 0.063
80
PYR013 Pyruvate Kinase Deficiency 58 0.062
81
P MSC033 Muscle Disorders 52 0.062
82
P HYP729 Hypersensitivity Reaction Disease 43 0.062
83
MSC004 Muscle Tissue Disease 37 0.062
84
P HYP265 Hypotonia 39 0.062
85
PCK002 Pick Disease 68 0.061
86
ATX038 Ataxia and Polyneuropathy, Adult-Onset 25 0.061
87
P HYP024 Hypoparathyroidism 52 0.060
88
BNS002 Bone Structure Disease 36 0.060
89
CHL067 Cholecystitis 55 0.059
90
P PNT019 Pontocerebellar Hypoplasia 38 0.059
91
ANX002 Anxiety Disorder 66 0.057
92
P ENC004 Encephalitis 61 0.057
93
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 41 0.057
94
CRB039 Cerebrovascular Disease 63 0.057
95
DDN006 Duodenitis 40 0.056
96
RSP006 Respiratory System Disease 60 0.055
97
P ESP024 Esophagitis 59 0.055
98
STR067 Stroke, Ischemic 72 0.053
99
P OBS005 Obesity 91 0.051
100
CLC006 Calcinosis 49 0.051
101
c EPL037 Epileptic Encephalopathy, Early Infantile, 1 36 0.051
102
c SZR016 Seizures, Benign Familial Infantile, 2 22 0.051
103
c PSD066 Pseudohypoparathyroidism, Type Ib 52 0.050
104
P BLP003 Blepharospasm 42 0.050
105
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 21 0.050
106
SCK003 Sickle Cell Anemia 71 0.048
107
P THL005 Thalassemia 61 0.048
108
HMG005 Hemoglobinopathy 51 0.048
109
P MGR003 Migraine with Aura 49 0.048
110
PRN021 Paranasal Sinus Disease 48 0.048
111
LKC003 Leukocyte Disease 46 0.048
112
BSL009 Basal Ganglia Calcification 43 0.048
113
ADP007 Adie Pupil 35 0.048
114
SPS019 Spastic Paraparesis 34 0.048
115
HMD003 Hemidystonia 27 0.048
116
PSY012 Psychogenic Movement 22 0.048
117
P MDL005 Medulloblastoma 73 0.044
118
WST001 West Syndrome 58 0.044
119
CNS004 Constipation 56 0.044
120
MYL001 Myelitis 48 0.044
121
DYS073 Dysphagia 47 0.044
122
GDS001 Good Syndrome 46 0.044
123
CNT025 Central Pontine Myelinolysis 38 0.044
124
FCL011 Facial Nerve Disease 35 0.044
125
VSL002 Visual Epilepsy 33 0.044
126
HRL006 Harel-Yoon Syndrome 25 0.044
127
P MYP004 Myopathy 68 0.043
128
ALX003 Alexander Disease 65 0.043
129
P STR022 Stargardt Disease 56 0.043
130
P THY032 Thyroiditis 53 0.043
131
TRN015 Transient Cerebral Ischemia 53 0.043
132
P STR020 Strabismus 52 0.043
133
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 43 0.043
134
P BLD051 Blood Coagulation Disease 43 0.043
135
BRN080 Brain Ischemia 40 0.043
136
ARM002 Aromatic L-Amino Acid Decarboxylase Deficiency 39 0.043
137
WBR001 Weber Syndrome 36 0.043
138
c SZR020 Seizures, Benign Familial Infantile, 5 17 0.043
139
c DLT002 Dilated Cardiomyopathy 74 0.036
140
WLS001 Wilson Disease 73 0.036
141
P LFR001 Li-Fraumeni Syndrome 72 0.036
142
P LYN001 Lynch Syndrome 71 0.036
143
BRN028 Brain Cancer 67 0.036
144
ATT013 Attention Deficit-Hyperactivity Disorder 66 0.036
145
P PRD006 Prader-Willi Syndrome 65 0.036
146
CYS013 Cystinuria 63 0.036
147
P PLR004 Pleuropulmonary Blastoma 58 0.036
148
STT001 Status Epilepticus 58 0.036
149
P MTR004 Maturity-Onset Diabetes of the Young 57 0.036
150
P HYP060 Hyperinsulinism 57 0.036
151
P GRV001 Graves' Disease 57 0.036
152
SFT003 Soft Tissue Sarcoma 56 0.036
153
GST033 Gestational Diabetes 55 0.036
154
HYP266 Hypoxia 55 0.036
155
P INT143 Interstitial Cystitis 54 0.036
156
P OVR049 Ovarian Disease 54 0.036
157
P LMY004 Leiomyosarcoma 54 0.036
158
THL016 Thalassemias, Alpha- 53 0.036
159
THL018 Thalassemia Major 52 0.036
160
ABL002 Ablepharon-Macrostomia Syndrome 52 0.036
161
RNP001 Renpenning Syndrome 52 0.036
162
P NNT009 Neonatal Diabetes Mellitus 51 0.036
163
QDR001 Quadriplegia 51 0.036
164
VRR004 Verrucous Carcinoma 50 0.036
165
PRV006 Pervasive Developmental Disorder 50 0.036
166
c CNG464 Congenital Myopathy 50 0.036
167
c ADL023 Adult Medulloblastoma 49 0.036
168
PLM032 Pulmonary Blastoma 49 0.036
169
PRP016 Paraplegia 48 0.036
170
LRN003 Learning Disability 46 0.036
171
HYP043 Hyperandrogenism 46 0.036
172
MXD023 Mixed Cell Type Cancer 45 0.036
173
ANL017 Anal Squamous Cell Carcinoma 45 0.036
174
PRT003 Partington Syndrome 44 0.036
175
ANX004 Anoxia 44 0.036
176
CRB090 Cerebral Hypoxia 44 0.036
177
P MYT023 Myotonia Congenita 44 0.036
178
MCR018 Microcytic Anemia 44 0.036
179
KHL003 Kohlschutter-Tonz Syndrome 42 0.036
180
c RTN055 Retinitis Pigmentosa 26 42 0.036
181
FRG010 Fragile X Tremor/ataxia Syndrome 41 0.036
182
P FNG006 Feingold Syndrome 1 40 0.036
183
BSL006 Basaloid Squamous Cell Carcinoma 40 0.036
184
ALP093 Alpha-Thalassemia/mental Retardation Syndrome, Chromosome 16-Related 40 0.036
185
MYT011 Myotonia 40 0.036
186
HYD038 Hydrops Fetalis, Nonimmune 39 0.036
187
BLD054 Blood Protein Disease 39 0.036
188
c DBT049 Diabetes Mellitus, Insulin-Dependent, 13 39 0.036
189
HNZ001 Heinz Body Anemia 39 0.036
190
c DBT048 Diabetes Mellitus, Insulin-Dependent, 11 39 0.036
191
HMG025 Hemoglobin H Disease, Nondeletional 39 0.036
192
SPC003 Specific Developmental Disorder 38 0.036
193
c DBT082 Diabetes Mellitus, Insulin-Dependent, 12 38 0.036
194
c DBT058 Diabetes Mellitus, Insulin-Dependent, 7 37 0.036
195
HYP026 Hypoglycemic Coma 37 0.036
196
c DBT038 Diabetes Mellitus, Insulin-Dependent, 5 36 0.036
197
OHD004 Ohdo Syndrome 36 0.036
198
c DBT054 Diabetes Mellitus, Insulin-Dependent, 24 36 0.036
199
CLR011 Clear Cell Ependymoma 35 0.036
200
BCK003 Background Diabetic Retinopathy 35 0.036
201
P EXT032 Extraosseous Osteosarcoma 34 0.036
202
RBS002 Rubeosis Iridis 34 0.036
203
HYP110 Hyperproinsulinemia 33 0.036
204
IMM039 Immune Hydrops Fetalis 33 0.036
205
HYP001 Hypochromic Microcytic Anemia 33 0.036
206
P PRD037 Periodontal Ehlers-Danlos Syndrome 31 0.036
207
SHP003 Shapiro Syndrome 30 0.036
208
SYN057 Syndromic Intellectual Disability 29 0.036
209
ISC003 Ischemic Fasciitis 29 0.036
210
MTH064 Methemoglobinemia, Beta-Globin Type 29 0.036
211
NRG003 Neurogenic Arthropathy 28 0.036
212
c PLZ002 Pelizaeus-Merzbacher-Like Disease 27 0.036
213
IMM002 Immature Cataract 26 0.036
214
P PHT010 Photoparoxysmal Response 1 26 0.036
215
c ALB016 Albinism, Oculocutaneous, Type Vii 25 0.036
216
c ERL003 Early Onset Absence Epilepsy 24 0.036
217
NNS031 Non-Syndromic Intellectual Disability 24 0.036
218
MCH006 Mechanical Strabismus 22 0.036
219
NNS032 Non-Syndromic X-Linked Intellectual Disability 22 0.036
220
MND006 Mondor Disease 22 0.036
221
c CRN174 Coronary Heart Disease 2 21 0.036
222
c EPL153 Epileptic Encephalopathy, Early Infantile, 29 21 0.036
223
XLN224 X-Linked Non-Specific Intellectual Disability 19 0.036
224
IQS001 Iqsec2 17 0.036
225
FMR005 Fmr1-Related Disorders 10 0.036
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